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Merck
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Key Documents

A38002

Sigma-Aldrich

4′-Aminoacetophenone

99%

동의어(들):

4-Acetylaniline

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About This Item

Linear Formula:
H2NC6H4COCH3
CAS Number:
Molecular Weight:
135.16
Beilstein:
471493
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

99%

형태

powder

bp

293 °C (lit.)

mp

103-107 °C (lit.)

SMILES string

CC(=O)c1ccc(N)cc1

InChI

1S/C8H9NO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,9H2,1H3

InChI key

GPRYKVSEZCQIHD-UHFFFAOYSA-N

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관련 카테고리

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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문서 라이브러리 방문

이미 열람한 고객

Anne Ly et al.
Organic & biomolecular chemistry, 3(5), 917-923 (2005-02-26)
The most easily oxidized sites in DNA are the guanine bases, and major intermediates produced by the direct effect of ionizing radiation (ionization of the DNA itself) are electron deficient guanine species. By means of a radiation chemical method (gamma-irradiation
Dominik Cincić et al.
Acta crystallographica. Section C, Crystal structure communications, 64(Pt 4), o226-o229 (2008-04-09)
In the title compounds, 4-carboxyanilinium bromide, C(7)H(8)NO(2)(+) x Br(-), (I), and 4-acetylanilinium bromide, C(8)H(10)NO(+) x Br(-), (II), each asymmetric unit contains a discrete cation with a protonated amino group and a halide anion. Both crystal structures are characterized by two-dimensional
O A Aleksintseva et al.
Antibiotiki, 27(7), 493-495 (1982-01-01)
The effect of p-aminobenzoic acid on the biosynthesis of levorin was studied. It was shown that in the presence of exogenic p-aminobenzoic acid the antibiotic activity increased by 11 per cent. The acid added was transformed into p-aminoacetophenone which was
O A Aleksintseva et al.
Antibiotiki, 26(8), 566-570 (1981-08-01)
A method for spectrophotometric determination of p-aminoacetophenone (p-AAP) in the mycelium and fermentation broth filtrates of organisms producing polyenic macrolide antibiotics is described. The level of p-AAP accumulation was studied as applicable to the biosynthesis of levorin, a polyenic antibiotic
O Raatikainen et al.
Journal of chromatography, 585(2), 247-254 (1991-11-01)
A high-performance liquid chromatographic (HPLC) method for the determination of the aromaticity of heptaene polyene antibiotics has been developed. The released aromatic moiety of the heptaene polyenes aureofungin, candicidin, candimycin, hamycin and trichomycin was assayed after alkaline hydrolysis. The presence

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